By the same authors

From the same journal

A NEW ROUTE TO 2E,4E-DIENALS FROM ORGANOMETALLIC REAGENTS VIA A 5-CARBON HOMOLOGATION PROCESS

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Publication details

JournalSynlett
DatePublished - Dec 1991
Issue number12
Number of pages3
Pages (from-to)898-900
Original languageEnglish

Abstract

A new procedure for the preparation of 2E,4E-dienals 4 is described based on the addition of organometallic reagents to silylated glutaconaldehyde 2 [(2E,4E)-5-trialkylsiloxy-2,4-pentadienal] as a five-carbon synthon. Application of the methodology to the synthesis of two dienamide natural products (pellitorine and sarmentine) are discussed.

    Research areas

  • CARBONYL-COMPOUNDS, ALDEHYDES

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